Synthesis of JP-10 analogues high-density fuels via one-pot Diels-Alder/ hydrodeoxygenation reaction

被引:7
|
作者
Xie, Junjian [1 ,2 ]
Zhang, Jun [1 ,2 ]
Wang, Xiaoyu [3 ,5 ]
Xie, Jiawei [4 ]
Yang, Bo [1 ,2 ]
Liang, Yuxuan [1 ,2 ]
Zou, Ji-Jun [5 ]
Zhang, Qiuyu [1 ]
机构
[1] Northwestern Polytech Univ, Sch Chem & Chem Engn, Xian 710072, Peoples R China
[2] Northwestern Polytech Univ Shenzhen, Res & Dev Inst, Shenzhen 518057, Peoples R China
[3] Beijing Inst Aerosp Testing Technol, Beijing Key Lab Res & Applicat Aerosp Green Propel, Beijing 100074, Peoples R China
[4] Sichuan Univ, Inst New Energy & Low Carbon Technol, Chengdu 610065, Peoples R China
[5] Tianjin Univ, Sch Chem Engn & Technol, Tianjin 300072, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
JP-10; fuel; High-density fuel; Cellulosic furans; Solid acid catalyst; Diels-Alder reaction; SELECTIVE PRODUCTION; CONVERSION; AROMATICS; CATALYST; ETHANOL; BIOMASS; JET;
D O I
10.1016/j.fuel.2023.130738
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
JP-10 is the most widely used petroleum based fuel in military aircraft due to its high energy density and excellent cryogenic properties. However, the high price and low availability limit its application in civil aviation. Herein, JP-10 analogues fuel was first synthesized via one-pot Diels-Alder/hydrodeoxygenation reaction using biomass-derived furans and petroleum-derived norbornene. H beta zeolite with Si/Al ratio of 25 exhibits the best catalytic performance (yield of 75.9 %) for Diels-Alder reaction ascribed to its large surface area and high acid concentration, especially the high ratio of Bronsted/Lewis acid sites. Kinetics research indicates that Diels-Alder reaction of norbornene and 2-methylfuran shows the apparent activation energy of 45.67 kJ/mol, much lower than that of norbornene dimerization (52.48 kJ/mol) and 2-methylfuran trimerization (63.61 kJ/mol). Importantly, the synthesized fuel has much higher density, volumetric neat heat of combustion and better cryogenic viscosity (0.943 g mL-1, 40.39 MJ/L and 12.9 mm2 s-1 at-40 degrees C) than classic JP-10 fuel (0.936 g mL-1, 39.41 MJ/L and 18.6 mm2 s-1 at-40 degrees C). This work provides an efficient and promising route to produce highperformance JP-10 fuel alternatives through co-conversion of biomass and petroleum derivatives.
引用
收藏
页数:8
相关论文
共 50 条
  • [21] Synthesis of high-density liquid fuel via Diels-Alder reaction of dicyclopentadiene and lignocellulose-derived 2-methylfuran
    Xie, Junjian
    Zhang, Xiangwen
    Liu, Yakun
    Li, Zheng
    Xiu-tian-feng, E.
    Xie, Jiawei
    Zhang, Yong-Chao
    Pan, Lun
    Zou, Ji-Jun
    CATALYSIS TODAY, 2019, 319 : 139 - 144
  • [22] An efficient one-pot synthesis of tetrahydroquinoline derivatives via an aza Diels-Alder reaction mediated by CAN in an aqueous medium and oxidation to heteroaryl quinolines
    Savitha, G.
    Perumal, P. T.
    TETRAHEDRON LETTERS, 2006, 47 (21) : 3589 - 3593
  • [23] Synthesis of Four Illudalane Sesquiterpenes Utilizing a One-Pot Diels-Alder/Oxidative Aromatization Sequence
    Xun, Miao-Miao
    Bai, Yunli
    Wang, Yanhong
    Hu, Zhiyong
    Fu, Kai
    Ma, Wenbing
    Yuan, Changchun
    ORGANIC LETTERS, 2019, 21 (17) : 6879 - 6883
  • [24] One-pot synthesis of pyridine derivatives via diels-alder reactions of 2,4-dimethyl-5-methoxyoxazole
    Bondock, S
    HETEROATOM CHEMISTRY, 2005, 16 (01) : 49 - 55
  • [25] One pot stimuli-responsive linear waterborne polyurethanes via Diels-Alder reaction
    Aizpurua, June
    Martin, Loli
    Formoso, Elena
    Gonzalez, Alba
    Irusta, Lourdes
    PROGRESS IN ORGANIC COATINGS, 2019, 130 : 31 - 43
  • [26] Efficient one-pot synthesis of benzopyranobenzopyrans and naphthopyranobenzopyrans by domino aldol-type reaction/hetero Diels-Alder reaction of resorcinols and naphthols
    Lee, Yong Rok
    Kim, Yun Mi
    Kim, Sung Hong
    TETRAHEDRON, 2009, 65 (01) : 101 - 108
  • [27] A one-pot synthetic approach to the functionalized isomeric ellipticine derivatives through an imino Diels-Alder reaction
    Gaddam, Vikram
    Nagarajan, Rajagopal
    TETRAHEDRON LETTERS, 2009, 50 (11) : 1243 - 1248
  • [28] DIENOPHILIC ACTIVITY OF VINYLDICHLOROBORANES AND THEIR USE AS PARTNERS IN DIELS-ALDER REDUCTIVE ALKYLATION OF AZIDES IN A ONE-POT REACTION
    NORET, N
    YOUSSOFI, A
    CARBONI, B
    VAULTIER, M
    JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1992, (16) : 1105 - 1107
  • [29] Ball-milling Synthesis of Tetrahydroquinolinesvia'One-pot' Three-component Diels-Alder Reaction Catalyzed by Phosphotungstic Acid
    Wang Zeyou
    Shen Guodong
    Huang Xianqiang
    Gong Shuwen
    Yang Bingchuan
    Sun Zhenzhen
    Zhang Zuhao
    Liu Wanxing
    CHEMICAL RESEARCH IN CHINESE UNIVERSITIES, 2020, 36 (05) : 835 - 842
  • [30] Substituent-controlled domino-Knoevenagel-hetero Diels-Alder reaction-a one-pot synthesis of polycyclic heterocycles
    Maiti, Sourav
    Panja, Suman Kalyan
    Bandyopadhyay, Chandrakanta
    TETRAHEDRON, 2010, 66 (38) : 7625 - 7632